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Malotilate is hepatotrophic drug which can selectively inhibit the 5-lipoxygenase, whereas both the 12- and the 15-lipoxygenase pathways were stimulated, with antifibrotic and hepatoprotective properties.
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CSNpharm
Malotilate is hepatotrophic drug which can selectively inhibit the 5-lipoxygenase, whereas both the 12- and the 15-lipoxygenase pathways were stimulated, with antifibrotic and hepatoprotective properties.
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CSNpharm
Malotilate is hepatotrophic drug which can selectively inhibit the 5-lipoxygenase, whereas both the 12- and the 15-lipoxygenase pathways were stimulated, with antifibrotic and hepatoprotective properties.
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CSNpharm
Malotilate is hepatotrophic drug which can selectively inhibit the 5-lipoxygenase, whereas both the 12- and the 15-lipoxygenase pathways were stimulated, with antifibrotic and hepatoprotective properties.
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CSNpharm
Maltitol is a sugar alcohol (polyol) used as a sugar substitute. It is especially useful in the production of sweets, including sugarless hard candies, chewing gum, chocolates.
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CSNpharm
Maltol is used as a flavour enhancer or flavouring agent that can be found in various foods like milk, breads and heated butter etc. Maltol also has a role as a metabolite.
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CSNpharm
Maltol is used as a flavour enhancer or flavouring agent that can be found in various foods like milk, breads and heated butter etc. Maltol also has a role as a metabolite.
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MnCl2 inhibits proliferation in a dose- and time-dependent manner, induces G0/G1 and S phase arrest and apoptosis in A549 cells.
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MnCl2 inhibits proliferation in a dose- and time-dependent manner, induces G0/G1 and S phase arrest and apoptosis in A549 cells.
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Mangiferin is the predominant constituent of extracts of the mango plant Mangifera Indica L. with potential antidiabetic activity.
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CSNpharm
Mangiferin is the predominant constituent of extracts of the mango plant Mangifera Indica L. with potential antidiabetic activity.
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CSNpharm
Mangiferin is the predominant constituent of extracts of the mango plant Mangifera Indica L. with potential antidiabetic activity.
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Manninotriose is an important player in the RFO (Raffinose family oligosaccharides) metabolism of red dead deadnettle with potential effect to improve the side effects of MTX for ALL treatment.
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CSNpharm
Manninotriose is an important player in the RFO (Raffinose family oligosaccharides) metabolism of red dead deadnettle with potential effect to improve the side effects of MTX for ALL treatment.
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CSNpharm
Manninotriose is an important player in the RFO (Raffinose family oligosaccharides) metabolism of red dead deadnettle with potential effect to improve the side effects of MTX for ALL treatment.
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Maohuoside A, a natural product isolated and purified from the roots of Epimedium brevicornu Maxim, seems to enhance the osteogenesis of rMSC and bone marrow-derived mesenchymal stem cells at least partly via the BMP and MAPK signaling pathways and bone morphogenetic protein signalling, respectively.
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CSNpharm
Maohuoside A, a natural product isolated and purified from the roots of Epimedium brevicornu Maxim, seems to enhance the osteogenesis of rMSC and bone marrow-derived mesenchymal stem cells at least partly via the BMP and MAPK signaling pathways and bone morphogenetic protein signalling, respectively.
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Maprotiline HCl is a bridged-ring tetracyclic antidepressant with adrenergic activity and sedative properties, exerting its effect by blocking the re-uptake of norepinephrine, thereby increasing the synaptic concentration of norepinephrine in the central nervous system and subsequently prolonging the action of norepinephrine on central receptors.
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Maprotiline HCl is a bridged-ring tetracyclic antidepressant with adrenergic activity and sedative properties, exerting its effect by blocking the re-uptake of norepinephrine, thereby increasing the synaptic concentration of norepinephrine in the central nervous system and subsequently prolonging the action of norepinephrine on central receptors.
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Maribavir is a potent inhibitor of histone phosphorylation catalyzed by wild-type pUL97 in vitro, with an IC50 of 3 nM. Maribavir has potent antiviral activity against HCMV and Epstein-Barr virus (EBV).
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Maribavir is a potent inhibitor of histone phosphorylation catalyzed by wild-type pUL97 in vitro, with an IC50 of 3 nM. Maribavir has potent antiviral activity against HCMV and Epstein-Barr virus (EBV).
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CSNpharm
Maribavir is a potent inhibitor of histone phosphorylation catalyzed by wild-type pUL97 in vitro, with an IC50 of 3 nM. Maribavir has potent antiviral activity against HCMV and Epstein-Barr virus (EBV).
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CSNpharm
Maribavir is a potent inhibitor of histone phosphorylation catalyzed by wild-type pUL97 in vitro, with an IC50 of 3 nM. Maribavir has potent antiviral activity against HCMV and Epstein-Barr virus (EBV).
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CSNpharm
Maribavir is a potent inhibitor of histone phosphorylation catalyzed by wild-type pUL97 in vitro, with an IC50 of 3 nM. Maribavir has potent antiviral activity against HCMV and Epstein-Barr virus (EBV).
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CSNpharm
Maribavir is a potent inhibitor of histone phosphorylation catalyzed by wild-type pUL97 in vitro, with an IC50 of 3 nM. Maribavir has potent antiviral activity against HCMV and Epstein-Barr virus (EBV).
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Marimastat is a competitive and broad-spectrum MMP inhibitor with IC50 values of 3, 5, 6, 9 and 13 nM for MMP-9, MMP-1, MMP-2, MMP-14 and MMP-7, respectively.
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CSNpharm
Marimastat is a competitive and broad-spectrum MMP inhibitor with IC50 values of 3, 5, 6, 9 and 13 nM for MMP-9, MMP-1, MMP-2, MMP-14 and MMP-7, respectively.
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CSNpharm
Marimastat is a competitive and broad-spectrum MMP inhibitor with IC50 values of 3, 5, 6, 9 and 13 nM for MMP-9, MMP-1, MMP-2, MMP-14 and MMP-7, respectively.
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CSNpharm
Marimastat is a competitive and broad-spectrum MMP inhibitor with IC50 values of 3, 5, 6, 9 and 13 nM for MMP-9, MMP-1, MMP-2, MMP-14 and MMP-7, respectively.
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